GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc02869 in Pseudomonas stutzeri RCH2

Align N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized)
to candidate GFF1860 Psest_1899 ABC-type sugar transport systems, ATPase components

Query= reanno::Phaeo:GFF2754
         (331 letters)



>FitnessBrowser__psRCH2:GFF1860
          Length = 390

 Score =  314 bits (804), Expect = 3e-90
 Identities = 172/367 (46%), Positives = 233/367 (63%), Gaps = 38/367 (10%)

Query: 1   MTALQLTNVCKSFGPVEV--LKDINLTVEDGEFVVFVGPSGCGKSTLLRVISGLEDATAG 58
           M +L+L NV KS+G  ++  LKDI L ++ GEF++ VGPSGCGKSTL+  I+GLE+ T G
Sbjct: 1   MASLELRNVQKSYGNSQIATLKDIALKIDAGEFLILVGPSGCGKSTLMNCIAGLENITGG 60

Query: 59  EISIGGQTVTTTPPAKRGIAMVFQSYALYPHLSVRENMALALKQERQPKEEIAARVAEAS 118
           EI + G+ ++   P  R IAMVFQSYALYP +SVR+N+A  LK  + P  +I   VA  +
Sbjct: 61  EILVDGEDISQASPKDRDIAMVFQSYALYPTMSVRDNIAFGLKMRKVPAAKIEEEVARVA 120

Query: 119 RMLSLEDYLDRRPSELSGGQRQRVAIGRAVVREPKLFLFDEPLSNLDAALRMNTRLEIAR 178
           ++L +E  L+R+PS+LSGGQ+QRVA+GRA+ R PK++LFDEPLSNLDA LR+  R EI  
Sbjct: 121 KLLQIEPLLERKPSQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEIKL 180

Query: 179 LHRQLSASMIYVTHDQIEAMTLADKIVVLRDGRIEQVGTPMELYNNPANRFVAEFIGAPA 238
           +H++L  + +YVTHDQIEAMTL DK+ V++DG I+Q GTP E+YNNPAN FVA FIG+P 
Sbjct: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGVIQQFGTPHEIYNNPANLFVASFIGSPP 240

Query: 239 MNFVPAQRLGGNPGQFI-----------------------------GIRPEYARISPVG- 268
           MNFVP  R+    G+++                             GIRPE   ++P G 
Sbjct: 241 MNFVPL-RIRQRDGRWVGVLNSEQGSCELPLPITSDDGLRDRELILGIRPEQIGLAPAGS 299

Query: 269 ---PLAGEVIHVEKLGGDTNILVDMGEDLTFTARLFGQHDTNVGETLQFDFDPANCLSFD 325
               LA ++  VE  G DT ++  + + +    RL       VGETL   FDP   L FD
Sbjct: 300 ADFSLAVDIEVVEPTGPDTLVVFTLNQ-VKACCRLAPDQAPRVGETLNLQFDPRRALLFD 358

Query: 326 -EAGQRI 331
            + G+R+
Sbjct: 359 AQTGERL 365


Lambda     K      H
   0.320    0.137    0.391 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 374
Number of extensions: 8
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 331
Length of database: 390
Length adjustment: 29
Effective length of query: 302
Effective length of database: 361
Effective search space:   109022
Effective search space used:   109022
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory